Search Results (31)

The pancreas is an organ with two functions: endocrine and exocrine. The proper functioning of the pancreas depends on many factors. One of these is trace elements—precise control of trace element homeostasis is important for both the endocrine and exocrine parts. This review provides a comprehensive summary of current knowledge regarding the role of trace elements: iron (Fe), copper (Cu), cobalt (Co), iodine (I), manganese (Mn), zinc (Zn), silver (Ag), cadmium (Cd), mercury (Hg), lead (Pb), and selenium (Se) in pancreatic physiology and their influence on the pathogenesis of key diseases of this organ, such as diabetes (DM), acute (AP) and chronic pancreatitis (CP), autoimmune pancreatitis (AIP), and pancreatic cancer (PC). Trace elements, including Fe, Cu, Zn, Se, and Mn, play a fundamental role in maintaining endocrine and exocrine homeostasis, participating in insulin synthesis, stabilizing digestive enzymes, and the functioning of antioxidant systems. It has been demonstrated that disturbances in their concentrations lead to the activation of pathological molecular pathways, including oxidative stress, chronic inflammation, and beta-cell apoptosis. In the context of diabetes, excess Fe promotes ferroptosis, whilst exposure to heavy metals such as Cd, Pb, and Hg induces insulin resistance and pancreatic islet dysfunction. In the course of pancreatitis, elements such as Zn and Se exhibit protective potential by stabilizing tissue barriers, whereas toxic metals impair ion transport, exacerbating fibrotic processes. Furthermore, analysis of available data indicates a significant association between heavy metal accumulation and pancreatic carcinogenesis, driven by DNA damage and oncogene modulation. Understanding pancreatic metallomics opens new prospects for early diagnosis, environmental prevention, and the development of targeted therapeutic strategies that restore the body’s micronutrient balance. Full article

The current research first investigates the flow in the fractional order of a vertical artery with atherosclerosis using a Casson-based penta-hybrid nanofluid. Gold (Au), copper (Cu), silver (Ag), magnesium oxide (MgO), and alumina (Al₂O₃) nanoparticles are dispersed in blood to make the hybrid nanofluid. It is assumed that the flow is very pulsatile. The mathematical model is constructed by using differential forms of the conservation laws of mass, momentum, energy, and irreversibility analysis. By applying the mild stenosis approximation, the governing equations are transformed into dimensionless form. To generalize the classical model to its fractional counterpart, the Caputo–Fabrizio fractional derivative (C-FFD) is employed. Closed-form solutions for the velocity and temperature fields are realized by the joint application of the Laplace and Hankel transforms. The impact of essential physical parameters on velocity, temperature, and entropy generation is displayed through figures. The physical significance of enhanced thermal characteristics is shown, emphasizing their potential relevance to thermal regulation, targeted drug delivery, and minimization of irreversible energy losses in biomedical flow systems. The velocity profile elevates with the increase in the Casson parameter, while the temperature drops as the fractional-order parameter rises. Entropy generation is observed to amplify with the increasing values of the thermodynamic parameter in question, whereas an opposite tendency is seen for the Bejan number. The Bejan number decreases as the control parameter becomes higher. The novelty of the present investigation lies in the simultaneous incorporation of Caputo–Fabrizio fractional dynamics, penta-hybrid nanoparticle suspension, and entropy generation analysis in a stenosed arterial configuration. Unlike existing fractional Casson blood flow models that primarily focus on single or hybrid nanofluids, the present framework highlights the synergistic enhancement of thermal transport and irreversibility control achieved through penta-hybrid nanoparticles, which may be relevant for advanced biomedical and targeted therapeutic applications. Full article

Skin cancer (SC) is the most prevalent malignancy worldwide, with subtypes varying in aggressiveness: basal cell carcinoma tends to be locally invasive, squamous cell carcinoma has a higher metastatic risk, and melanoma remains the deadliest form. Current treatments such as surgery, radiotherapy, and systemic chemotherapy are associated with aesthetic and functional morbidity, recurrence, and/or systemic toxicity. Although targeted therapies and immunotherapies offer clinical benefits, their high cost and limited accessibility underscore the need for innovative, affordable alternatives. Metal-based compounds (metallopharmaceuticals) are promising anticancer agents due to their ability to induce oxidative stress, modulate redox pathways, and interact with DNA. However, clinical translation has been limited by poor aqueous solubility, rapid degradation, and low skin permeability. This review discusses the most recent preclinical findings on gold, silver, platinum, palladium, ruthenium, vanadium, and copper complexes, mainly in topical and systemic treatments of SC. Advances in chemical and physical enhancers, such as hydrogels and microneedles, and in drug delivery systems, including bacterial nanocellulose membranes and nanoparticles, as well as liposomes and micelles, for enhancing skin permeation and protecting the integrity of metal complexes are also discussed. Additionally, we examine the contribution of photodynamic therapy to SC treatment and the use of mathematical and computational modeling to simulate skin drug transport, predict biodistribution, and support rational nanocarrier design. Altogether, these strategies aim to bridge the gap between physicochemical innovation and clinical applicability, paving the way for more selective, stable, and cost-effective SC treatments. Full article

European energy and climate policies have enabled reductions in greenhouse gas emissions across many sectors, with transport standing out as an exception. In this area, one of the most promising solutions is the electrification of vehicles. In urban contexts, the shift towards electrifying transport—particularly local public transport (LPT)—can yield significant benefits, especially when paired with an increasingly decarbonized electricity mix, effectively reducing tailpipe emissions of both greenhouse gases and other pollutants. Nevertheless, it is essential to assess whether eliminating tailpipe emissions simply shifts environmental impacts to other stages of a vehicle’s life cycle. The Life Cycle Assessment (LCA), employing a comprehensive cradle-to-grave approach, serves as the principal tool for such evaluations. In this framework, this study focuses on the Italian situation by using a dynamic LCA for the electricity mix. Results show that the electric bus reduces the impact on climate change (28.5 gCO₂eq/pkm vs. 66.7 gCO₂eq/pkm for Diesel, −57%), acidification, photochemical ozone formation, particulate matter, and the use of fossil resources. However, it presents higher impacts in terms of human toxicity (both carcinogenic and non-carcinogenic) and the use of mineral and metal resources, mainly due to battery production and the use of metals such gold, silver, and copper. Full article

The nourishment of the human population depends on a handful of staple crops, such as maize, rice, wheat, soybeans, potatoes, tomatoes, and cassava. However, all crop plants are affected by at least one virus causing diseases that reduce yield, and in some parts of the world, this leads to food insecurity. Conventional management practices need to be improved to incorporate recent scientific and technological developments such as antiviral gene silencing, the use of double-stranded RNA (dsRNA) to activate an antiviral response, and nanobiotechnology. dsRNA with antiviral activity disrupt viral replication, limit infection, and its use represents a promising option for virus management. However, currently, the biggest limitation for viral diseases management is that dsRNA is unstable in the environment. This review is focused on the potential of nanoparticles and nanocarriers to deliver dsRNA, enhance stability, and activate antiviral gene silencing. Effective carriers include metal-based nanoparticles, including silver, zinc oxide, and copper oxide. The stability of dsRNA and the efficiency of gene-silencing activation are enhanced by nanocarriers, including layered double hydroxides, chitosan, and carbon nanotubes, which protect and transport dsRNA to plant cells. The integration of nanocarriers and gene silencing represents a sustainable, precise, and scalable option for the management of viral diseases in crops. It is essential to continue interdisciplinary research to optimize delivery systems and ensure biosafety in large-scale agricultural applications. Full article

The development of thin-film organic solar cells (TFOSCs) is pivotal for advancing sustainable energy technologies because of their potential for low-cost, lightweight, and flexible photovoltaic applications. In this study, silver-doped copper sulfide (CuS/Ag) metal nanoparticles (MNPs) were successfully synthesized via a wet chemical method. These CuS/Ag MNPs were incorporated at varying concentrations into a poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) blend, serving as the active layer to enhance the photovoltaic performance of the TFOSCs. The fabricated TFOSC devices were systematically evaluated based on the optical, electrical, and morphological characteristics of the active layer. By varying the concentration of CuS/Ag MNPs, the influence of nanoparticle doping on photocurrent generation was investigated. The device incorporating 1% CuS/Ag MNPs exhibited the highest power conversion efficiency (PCE) of 5.28%, significantly outperforming the pristine reference device, which achieved a PCE of 2.53%. This enhancement is attributed to the localized surface plasmon resonance (LSPR), which augments charge transport and increases optical absorption. The CuS/Ag MNPs were characterized using ultraviolet–visible (UV-Vis) absorption spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and energy-dispersive dispersion (EDX) analysis. These findings underscore the potential of CuS/Ag MNPs in revolutionizing TFOSCs, paving the way for more efficient and sustainable solar energy solutions. Full article

This study identified an oxidase-positive protein in the plasma membrane fraction of the C. elegans N2 strain. The protein with a molecular weight of approximately 85 kDa reacted with antibodies against human and mouse, but not rat, ceruloplasmin and exhibited oxidase activity. Bioinformatic analysis revealed that the F21D5.3 protein possesses four copper-binding sites, similar to those in other multicopper oxidases (MCOs), and plastocyanin-like domains characteristic of MCOs. However, neither an iron-binding domain nor ferroxidase activity, typical features of MCOs, were detected through in silico analysis and or in-gel assays. Despite the absence of ferroxidase activity, these findings suggest that the protein may be the product of the F21D5.3 gene, an ortholog of MCOs in C. elegans. Heat map analysis indicated F21D5.3 expression in the entero-rectal valve cells and both the anterior and posterior intestines. Among the genes associated with copper transport, only cua-1 exhibited a similar expression pattern. In the C. elegans cua-1^H828Q strain, which mimics a mutation in human ATP7B linked to Wilson’s disease (WD), oxidase activity was also observed. Notably, both strains showed reduced oxidase activity when cultured with silver nanoparticles (AgNPs). These findings highlight the potential of the cua-1^H828Q strain as a model for studying copper and iron metabolism and for developing therapeutic strategies for WD. Full article

Metallic lithium anodes possess the lowest redox potential (−3.04 V vs. SHE) and an ultra-high theoretical capacity (3860 mAh g⁻¹, 2061 mAh cm⁻³). However, during electrochemical cycling, lithium metal tends to plate unevenly, leading to the formation of lithium dendrites. Moreover, severe electrochemical corrosion occurs at the interface between metallic lithium and traditional copper foil current collectors. To address these issues, we selected corrosion-resistant carbon paper as a lithium metal host and modified a uniform distribution of silver nanoparticles and a F-doped amorphous carbon structure as a highly lithiophilic F-CP@Ag host to enhance lithium-ion transport kinetics and achieve improved affinity with lithium metal. The silver nanoparticles reduced the lithium nucleation energy barrier, while F doping resulted in a LiF-rich solid electrolyte interphase that better accommodated volume changes in lithium metal. These two strategies worked together to ensure uniform and stable lithium metal plating/stripping on the F-CP@Ag host. Consequently, under the conditions of 1 mA cm⁻² and 1 mAh cm⁻², the symmetric cell exhibited stable cycling with a polarization voltage of 8 mV for up to 1400 h. This work highlights the corrosion problem of lithium metal on traditional copper foil current collectors and provides guidance for the long-term cycling stability of lithium metal anodes. Full article

A comprehensive X-ray topography analysis of two selected aluminum nitride (AlN) bulk crystals is presented. We compare surface inspection X-ray topography in back-reflection geometry with high-energy transmission topography in the Lang and Laue configuration using the monochromatic K_α1 excitation wavelength of copper, silver, and tungsten, respectively. A detailed comparison of the results allows the assessment of both the high- and low-energy X-ray topography methods with respect to performance and structural information, giving essential feedback for crystal growth. This is demonstrated for two selected AlN freestanding faceted crystals up to 8 mm in thickness grown in all directions using the physical vapor transport (PVT) method. Structural defects of all facets of the crystals are determined using the X-ray topography in back-reflection geometry. The mean threading dislocation densities are 480 ± 30 cm⁻² for both crystals of either the Al- or N-face. Clustering of dislocations could be observed. The m-facets show the presence of basal plane dislocations and their accumulation as clusters. The integral transmission topographs of the $10\overline{1}0$ (m-plane) reflection family show that basal plane dislocations of the screw type in ${\displaystyle \frac{1}{3}}⟨\overline{1}2\overline{1}0⟩$ directions decorate threading dislocation clusters. Three-dimensional section transmission topography reveals that the basal plane dislocation clusters mainly originate at the seed boundary and propagate in the ${\displaystyle \frac{1}{3}}⟨\overline{1}2\overline{1}0⟩$ direction along the growth front. In newly laterally grown material, the Borrmann effect has been observed for the first time in PVT-grown bulk AlN, indicating very high structural perfection of the crystalline material in this region. This agrees with a low mean FWHM of 10.6 arcsec of the $10\overline{1}0$ reflection determined through focused high-energy Laue transmission mappings. The latter method also opens the analysis of the $∆2\theta$-shift correlated to the residual stress distribution inside the bulk crystal, which is dominated by dislocation clusters. Contrary to Lang transmission topography, the de-focused high-energy Laue transmission penetrates the 8 mm-thick crystal enabling a defect analysis in the bulk. Full article

As a promising structure for fabricating inorganic—organic-based optoelectronic devices, metal—metallophthalocyanine (MPc) hybrid layers are highly important to be considered. The efficient charge injection and transport across the metal/MPc interface are strictly dependent on the precise molecular orientation of the MPcs. Therefore, the efficiency of MPc-based optoelectronic devices strictly depends on the adsorption and orientation of the organic MPc on the inorganic metal substrate. The current review aims to explore the effect of the terminated atoms or surface atoms as an internal stimulus on molecular adsorption and orientation. Here, we investigate the adsorption of five different phthalocyanine molecules—free-based phthalocyanine (H₂Pc), copper phthalocyanine (CuPc), iron phthalocyanine (FePc), cobalt phthalocyanine (CoPc), vanadyl phthalocyanine (VOPc)—on three metallic substrates: gold (Au), silver (Ag), and copper (Cu). This topic can guide new researchers to find out how molecular adsorbance and orientation determine the electronic structure by considering the surface–molecule interactions. Full article

This paper investigates the mineralogical and geochemical characteristics, as well as the possible sources, of gold, silver, platinum group elements (PGE), copper, and lead found in the beach sands along Egypt’s Mediterranean coast. Using scanning electron microscopy and electron probe micro-analysis, this study determines the morphology and micro-chemistry of separated grains to assess their economic potential and how various minerals respond to different transport distances. The analysis reveals that gold grains are of high purity (94.11 to 98.55 wt.%; average 96 wt.% Au) and are alloyed with Ag (1.28–2.32 wt.%) and Cu (0.16–3.15 wt.%). Two types of gold grains were identified, indicating differences in transport distances. Variations in morphology, surface features, inclusion types, rims, and chemistry of the native metals, including gold grains, suggest differences in composition, weathering degree, transport distance, deposit types, and host rocks. The average Ag concentration in gold grains (1.86 wt.%) suggests a link to mesothermal or supergene deposits. Most silver, copper, and lead grains are spherical, with some variations in shape. Silver grains have 71.66–95.34 wt.% Ag (avg. 82.67 wt.%). Copper grains have 92.54–98.42 wt.% Cu (avg. 94.22 wt.%). Lead grains contain 74.22–84.45 wt.% Pb (avg. 79.26 wt.%). The identified platinum group minerals (PGM) belong to the Pt–Fe alloys and sperrylite, both of which are PPGE-bearing minerals. These metals likely originate from the weathering of upstream Nile tributaries surrounded by igneous and metamorphic rocks from Ethiopian and Central African regions, with a minor contribution from the Egyptian Eastern Desert Mountains. Full article

This study focuses on advancing sweat management in clothing using low-current operating textile electroosmotic pumps, which could be beneficial for microenvironments with restricted ventilation, such as the one between the skin and protective wear. These systems, employing silver–copper fabric electrodes, a polycarbonate membrane with microchannels, and an adhesive web, enabled directed liquid transport. The critical role of the adhesive layer preparation is emphasized, often overlooked in previous research. Various adhesive perforations were tested for their impact on the flow under current action, both with and against gravity. Specific adhesive application techniques are proposed, found to significantly influence the flow rate and textile assembly cohesion. The custom setup yielded flow rates of up to 8.8 ± 0.08 mg min⁻¹ cm⁻², suitable for diverse human sweat rates. Optimization hinges on the delicate balance between binding and the active surface areas of the adhesive. Full article

The link between copper metabolism and tumor progression motivated us to use copper chelators for suppression of tumor growth. We assume that silver nanoparticles (AgNPs) can be used for lowering bioavailable copper. Our assumption is based on the ability of Ag(I) ions released by AgNPs in biological media and interfere with Cu(I) transport. Intervention of Ag(I) into copper metabolism leads to the replacement of copper by silver in ceruloplasmin and the decrease in bioavailable copper in the bloodstream. To check this assumption, mice with ascitic or solid Ehrlich adenocarcinoma (EAC) were treated with AgNPs using different protocols. Copper status indexes (copper concentration, ceruloplasmin protein level, and oxidase activity) were monitored to assess copper metabolism. The expression of copper-related genes was determined by real-time PCR in the liver and tumors, and copper and silver levels were measured by FAAS. Intraperitoneal AgNPs treatment beginning on the day of tumor inoculation enhanced mice survival, reduced the proliferation of ascitic EAC cells, and suppressed the activity of HIF1α, TNF-α and VEGFa genes. Topical treatment by the AgNPs, which was started together with the implantation of EAC cells in the thigh, also enhanced mice survival, decreased tumor growth, and repressed genes responsible for neovascularization. The advantages of silver-induced copper deficiency over copper chelators are discussed. Full article

Sulfides and selenides of copper and silver have been intensively studied, particularly as potentially efficient thermoelectrics. Ag${}_3$CuS${}_2$ (jalpaite) is a related material. However very little is known about its physical properties. It has been found that the compound undergoes several structural phase transitions, having the tetrahedral structural modification I4${}_1$/amd at room temperature. In this work, its band structure, phonon spectrum and thermoelectric properties were studied theoretically and experimentally. Seebeck coefficient, electrical conductivity and thermal conductivity were measured in a broad temperature range from room temperature to 600 K. These are the first experimental data on transport properties of jalpaite. Ab initio calculations of the band structure and Seebeck coefficient were carried out taking into account energy dependence of the relaxation time typical for the scattering of charge carriers by phonons. The results of the calculations qualitatively agree with the experiment and yield large values of the Seebeck coefficient characteristic for lightly doped semiconductor. The influence of intrinsic defects (vacancies) on the transport properties was studied. It was shown that the formation of silver vacancies is the most probable and leads to an increase of hole concentration. Using the temperature dependent effective potential method, the phonon spectrum and thermal conductivity at room temperature were calculated. The measurements yield low lattice thermal conductivity value of 0.5 W/(m K) at 300 K, which is associated with the complex crystal structure of the material. The calculated room temperature values of the lattice thermal conductivity were also small (0.14–0.2 W/(m K)). Full article

This paper reviews a procedure that allows for extracting primary photoelectron or Auger electron emissions from homogeneous isotropic samples. It is based on a quantitative dielectric description of the energy losses of swift electrons travelling nearby surfaces in presence of stationary positive charges. The theory behind the modeling of the electron energy losses, implemented in a freely available QUEELS-XPS software package, takes into account intrinsic and extrinsic effects affecting the electron transport. The procedure allows for interpretation of shake-up and multiplet structures on a quantitative basis. We outline the basic theory behind it and illustrate its capabilities with several case examples. Thus, we report on the angular dependence of the intrinsic and extrinsic Al 2s photoelectron emission from aluminum, the shake-up structure of the Ag 3d, Cu 2p, and Ce 3d photoelectron emission from silver, CuO and CeO₂, respectively, and the quantification of the two-hole final states contributing to the L₃M₄₅M₄₅ Auger electron emission of copper. These examples illustrate the procedure, that can be applied to any homogeneous isotropic material. Full article